Nerves and Action potentials Flashcards

1
Q

CNS glial (non neuronal) cells

A
  1. astrocytes
    –> secrete neurotrophic factors, regulate extracellular environment, neurotransmitter uptake and help form blood-brain barrier, source of neural stem cells, provides substrates for ATP production
  2. oligodendrocytes
    –> provides the myelin in the CNS
  3. microglial cells
    –> immune, uses phagocytosis as defence mechanism
  4. ependymal cells
    –> create barriers for compartmentalisation, source of neural stem cells
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2
Q

neurotrophic factors

A
  • it is responsible for guiding neurons, specifically their axons, to the correct target
  • promote the survival of neurons during development and throughout the lifespan
  • regeneration and sprouting of axons after damage.
    *
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3
Q

PNS glial (non neuronal) cells

A

schwann cells
–>produce myelin
satellite cells
–> support cell bodies

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4
Q

Structure and function of the anatomy of a Neuron

A

Dendrites: receive input signals or stimuli from other neurons or sensory cells.

Cell Body (Soma): contains the nucleus and other cellular organelles –> integrates the incoming signals received from dendrites and makes a decision on whether to generate an action potential.

Axon Hillock: a specialized region of the cell body.
–> It plays a critical role in determining whether an action potential is generated in the neuron. determines to check If the integrated signals does reach the threshold, for action potential to be initiated.

Axon: It transmits the signal along its length toward the synaptic terminals. Signal Transmission is Unidirectional Flow: starts at the dendrites, passes through the cell body, and travels along the axon to the synaptic terminals.

Synaptic Terminals: form synapses where axon terminal communicates with postsynpatic target cells ; neurotransmitters are released to transmit the signal to the next cell.

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5
Q

Describe the interrelationship of electrical, chemical and electrochemical gradients.

A

An electrochemical gradient is a combined force resulting from both the electrical gradient (voltage difference) and the chemical gradient (concentration difference) across a cell membrane.

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6
Q

Demonstrate an understanding of membrane potential and how it is generated.

A

At rest, the intracellular compartment (IC) is high in K+, and the extracellular compartment (EC) is high in Na+.

the IC compartment has a negative charge relative
to the EC compartment (-70mV; resting potential)

The membrane potential is affected by altering
membrane permeability to certain ions
If K + permeability increases, potential = more negative [K+ will flow out]
If Na+ permeability increases, potential = more positive [Na+ will flow in]

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7
Q

Describe the generation of a graded potential

A
  • any stimulus that can open gated ion channels in the cell membrane e.g. mechanical, chemical, or electrical.
  • occur locally and are confined to the specific region of the cell membrane where the stimulus is applied.
  • they do not propagate over long distances.

Graded potentials can be either depolarizations or hyperpolarizations:
Depolarization: an increase in positive charge inside the cell, (e.g., entry of Na+).
Hyperpolarization: a more negative charge inside the cell, (e.g., exit of K+).

Repolarization: return of the membrane potential to its resting state after a graded potential.

–> They are crucial for influencing the generation of action potentials in neurons.

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8
Q

Describe generation of an action potential

A

Action Potentials: when a graded potential reaches the axon hillock and depolarizes the membrane to a threshold level.

must be above ‘threshold’ in the trigger zone [needs to last longer to the site where it would be initiated, see if it is still above threshold = action potential]

capable of propagating over long distances along the axon.

Action potentials follow an all-or-none principle

Phases:
* Depolarization Phase
* Repolarization Phase
* Hyperpolarization (Afterpotential) Phas

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9
Q

key differences between the action and graded potential.

A

Propagation:
Graded potentials do not propagate over long distances and are confined to the site of stimulation/ action potential are capable of propagating over long distances along the axon.

All-or-None vs. Graded Responses:
Action potentials follow an all-or-none response, where reaching the threshold triggers a full action potential.
Graded potentials exhibit a graded response, with the magnitude of the response proportional to the strength of the stimulus.

Location:
Graded potentials occur at dendrites and cell bodies.
Action potentials are typically initiated at the axon hillock.

Graded potentials do not regenerate. This means that as the graded potential travels away from the site of the stimulus, its strength diminishes or decreases. The electrical signal weakens as it travels through the cell membrane, and its effects diminish over distance.

Action potentials have the ability to regenerate. This means that as the action potential travels along the axon, it maintains its strength and does not diminish due to the presence of voltage-gated ion channels along the axon. These channels open in response to the depolarization of the membrane, allowing the influx of ions and the propagation of the action potential. This process repeats along the length of the axon

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10
Q

Understand the concept of summation

A

The concept of summation in neuroscience refers to the combining of multiple graded potentials to reach the threshold for generating an action potential. There are two main types of summation: temporal summation and spatial summation.

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11
Q

describe the differences between temporal and spatial summation.

A

Temporal Summation: when two or more graded potentials arrive at the same location on the neuron’s membrane in rapid succession.
Same Location, Close in Timing:

The key characteristic of temporal summation is that the graded potentials are generated at the same synaptic input location, but they occur closely in time.
–> Each individual signal may be sub-threshold, but the cumulative effect of the signals, when combined in time, may lead to the generation of an action potential.

Spatial Summation: when two or more graded potentials, each generated at different synaptic input locations on the neuron’s membrane, arrive simultaneously.
Close in Location, Same Timing:
–> if the individual graded potentials are sub-threshold, their effects can add up spatially=an action potential will be generated.

Diff:
Temporal Summation: Graded potentials combine over time at the same synaptic input location.
Spatial Summation: Graded potentials combine simultaneously but at different synaptic input locations.

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12
Q

threshold def

A

Threshold is a depolarisation large enough to trigger
opening of voltage-gated Na + channels (~-60 to -55mV)

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13
Q

depolarisation def

A

a change in the membrane potential of a cell where the inside of the cell becomes less negative compared to the resting membrane potential.
= an influx of positive ions, typically sodium ions (Na+), making the membrane potential less negative or more positive.

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14
Q

repolarisation def

A

the process of restoring the membrane potential of a cell back to its resting state after depolarization or hyperpolarization [action potentials –> repolarization follows the depolarization phase]
= the efflux of ions that were responsible for depolarization, typically potassium ions (K+), allowing the cell to return to its resting membrane potential.

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15
Q

hyperpolarisation def

A

a change in the membrane potential of a cell, leading to an increase in the negativity of the inside of the cell compared to the resting membrane potential.
= an efflux of positive ions, often potassium ions (K+), or an influx of negative ions, such as chloride ions (Cl-).

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16
Q

Explain the absolute refractory period

A

Period when neuron does not respond normally to depolarising stimulus

Absolute refractory period:
All Na + channels are open (if the action potential is still ongoing) or inactivated (if the action potential has just occurred).
In either case, the channels are temporarily unavailable to respond to another depolarizing stimulus.
Action potential CANNOT fire

:Primarily during the depolarization, peak, and early repolarization phases.

17
Q

Explain the relative refractory period

A

Period when neuron does not respond normally to depolarising stimulus

Relative refractory period:
Na + channels begin to resume resting state
Action potential CAN fire but requires larger-than-normal stimulus to reach the threshold for generating an action potential.

:Mainly during the later repolarization and hyperpolarization phases.

18
Q

refractory period impact on action potential generation and propagation.

A

Prevention of Backward Propagation: ensures that the action potential travels only in one direction along the axon.

Control of Firing Frequency: neuron needs a recovery period before it can generate another action potential, preventing excessive firing and maintaining a regulated signaling system.

Response to Stimuli: relative refractory period allows the neuron to respond to strong stimuli, providing a mechanism for the modulation of signal strength based on the intensity of incoming signals.

19
Q

Describe the differences between continuous and saltatory propagation.

A

Axon Type:
c: smaller unmyelinated axons/ s: myelinated axons, especially those with larger diameters.

Speed:
c: slower/ s: faster as the action potential “jumps” between nodes of Ranvier.

Energy Efficiency:
c: requires more energy as ion movements occur along the entire length of the axon/s: more energy-efficient, with ion movements concentrated at the nodes of Ranvier.

Anatomy:
c: involves the entire axonal membrane/ s: involves the nodes of Ranvier and the myelinated regions between them.

20
Q

Identify the properties of an axon that can affect action potential conduction velocity.

A

Axon Diameter:
The larger the axon diameter, the lower the resistance to the flow of ions = faster

Myelination:
faster than unmyelinated axons : saltatory conduction.

Temperature:
increase conduction velocity = faster molecular movement and, consequently, quicker ion channel opening and closing. This results in an overall increase in conduction velocity.

Voltage-Gated Channels:
The speed at which voltage-gated sodium and potassium channels open and close affects the rate of action potential propagation. Axons with fast-opening channels may conduct signals more rapidly.

Myelin Thickness:
Thicker myelin allows for faster saltatory conduction = the thickness influences how quickly the action potential jumps between nodes of Ranvier.

Axon Length:
Longer axons = longer distance for the action potential to travel –> slower

21
Q

Continuous propagation.

A

Continuous propagation
Occurs in unmyelinated axons
Channels open sequentially –
Depolarisation of one region –> depolarisation of
adjacent region, and so on
Slow (~1 m/s)

22
Q

Saltatory propagation.

A

Saltatory propagation
Occurs in myelinated axons
Myelin sheath prevents current leak (insulator) [skips the local currents in adjacent sections]
Action potentials “jump” between Nodes of Ranvier
Fast (>100 m/s)

23
Q

Stages of an Action Potential

A
  1. resting membrane potential
  2. depolarising stimulus –> reaches threshold
  3. voltage gated Na+ channels are activated = influx of Na+ –> depolarisation
  4. Na+ channels close and opening of K+ channels = exit of K+ from cell to ECF
  5. K+ channels remain open –> hyperpolarisation
  6. voltage gated K+ channels close
  7. cell returns to normal ion permeability and resting membrane potential
24
Q

Propagation of an Action Potential

A
  1. graded potential above threshold reaches trigger zone
  2. voltage gated Na+ channels open and Na+ enters the axon
  3. Na+ depolarises the membrane and causes a local current flow, positive charge flows to adjacent sections of the axon
  4. adjacent sections also depolarise, process repeats itself
  5. previous segment goes through refractory period to ensure unidirectional propagation
25
Q

Classification of axons (fibres)

A

Type A Fibers:
Myelinated axons with a large diameter (4-20 μm)
fast conduction (>100 m/s) –> efficient transmission
Reserved for essential sensory and motor signaling crucial for survival.

Type B Fibers:
Myelinated axons with a smaller diameter (2-4 μm).
Show moderate conduction speed (~18 m/s).

Type C Fibers:
Unmyelinated axons with a small diameter (<2 μm).
Exhibit slow conduction speed (~1 m/s).

the reason not all are myelinated : While larger diameter and myelination contribute to faster conduction, they also increase the overall size or bulk of the axon.